Use of modified cells for the treatment of multiple sclerosis

ABSTRACT

The present invention describes blood cells chemically coupled with immunodominant myelin peptides and their use in the treatment of Multiple Sclerosis.

This application is a continuation-in-part of U.S. Ser. No. 12/740,502, filed Oct. 13, 2010, now issued as U.S. Pat. No. 8,673,293, which is a U.S. National Stage under §371 of PCT/EP2008/009204, filed Oct. 31, 2008, which applications claim priority to EP07075952.7, filed Oct. 31, 2007.

Multiple sclerosis (MS) is a devastating autoimmune inflammatory disease of the brain and spinal cord mainly affecting young adults.

Multiple sclerosis (MS) is the most frequent debilitating neurological disease of young adults in Europe (prevalFence 60-200/100,000, incidence 2-4/100,000), with half of patients needing a walking aid 10-15 years from onset of the disease. MS ranks second only to trauma in the age group of young adults with respect to socioeconomic costs. The symptoms of MS vary, depending on the location of lesions within the CNS, including focal weakness, sensory deficits, double vision, loss of vision, imbalance, fatigue, urinary and bowel dysfunction, sexual impairment and cognitive decline. In most patients the disease starts with a relapsing-remitting disease course (RR-MS), which is followed by a secondary progressive deterioration usually beginning about ten years after disease onset (SP-MS). The etiology is unknown, but it is well accepted that the damage in the central nervous system (CNS) results from an autoimmune attack against (auto) antigens within the myelin sheath. Currently approved therapies for MS involve various antigen-nonspecific immunomodulating or immunosuppressive strategies, which are only partially effective in that they prevent 30%-50% of relapses. Preventing progression of disability has not been consistently demonstrated for these therapies, yet. However, most current therapeutics need to be injected for long periods of time and are associated with considerable side effects. Particularly in a chronic disease as MS, therapy should aim to specifically delete or functionally inhibit pathogenic autoreactive cells without altering the “normal” immune system. This is of importance because global immunomodulation and/or immunesuppression come at the cost of inhibiting beneficial regulatory cells and immune cells that might serve protective functions. Thus the ideal treatment would be early intervention using an antigen-specific tolerance protocol that selectively targets both activated and naïve autoreactive T cells specific for multiple potential encephalitogenic epitopes that perpetuate the disease.

The mechanisms responsible for tissue damage in MS involve the activation of self-reactive T lymphocytes which attack proteins in the myelin sheath. Current therapies for MS inhibit the autoimmune response in a nonspecific manner, are only moderately effective and can have significant side effects. Based on success in pre-clinical experiments in animal models of MS, embodiments of the present application provide a new therapeutic strategy, which will specifically target only the autoreactive CD4+ T lymphocytes. Tolerance will be induced by a single administration of blood cells, in particular red blood cells (erythrocytes) or peripheral blood mononuclear cells (PBMCs) chemically coupled with a mixture of synthetic myelin antigens to which T cell responses are demonstrable in early MS patients. The therapy is exquisitely antigen-specific and renders autoreactive T cells non-functional or anergic.

The induction of tolerance to target autoantigens is a highly important therapeutic goal in autoimmune diseases. It offers the opportunity to attenuate specifically the pathogenic autoimmune response in an effective way with few side effects. To achieve this goal, embodiments of the present application provide a very promising tolerization strategy that employs autologous peptide-pulsed, fixed, antigen presenting cells as tolerogen. This therapy has proven excellent efficacy in animal models of MS and different T cell-mediated autoimmune diseases.

The therapy is based on systemic administration of blood cells chemically coupled with a cocktail of peptides containing at least five of eight immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀, MOG₃₅₋₅₅ and MBP₈₂₋₉₈), to which T cell responses are demonstrable in early RR-MS patients. Preferred is the use of six, seven, or eight of the named immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀, MOG₃₅₋₅₅ and MBP₈₂₋₉₈).

An alternative therapy is based on systemic administration of blood cells chemically coupled with a cocktail of peptides containing at least five of twenty immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆), to which T cell responses are demonstrable in early RR-MS patients. Preferred is the use of six, seven, eight or even more (up to 14, see table 5) of the named immunodominant myelin peptides (MBP₁₃₋₃₂, MBP 83-99, MBP 111-129, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆).

The blood cells may be autologous (relative to the treated subject) in case of peripheral blood mononuclear cells (PBMCs) and in case of red blood cells (erythrocytes) or the blood cells or may be allogeneic (relative to the treated subject) in case of red blood cells (erythrocytes).

Preferred blood cells are red blood cells (erythrocytes) and peripheral blood mononuclear cells (PBMCs). The preferred route for systemic administration is i.v. administration.

A preferred aspect of the invention is therefore a therapy based on systemic administration of autologous peripheral blood mononuclear cells chemically coupled with a cocktail containing at least five of eight immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀, MOG₃₅₋₅₅ and MBP₈₂₋₉₈), to which T cell responses are demonstrable in early RR-MS patients. Preferred is the use of six, seven or eight of the named immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀, MOG₃₅₋₅₅ and MBP₈₂₋₉₈).

A further preferred aspect of the invention is therefore a therapy based on systemic administration of red blood cells or erythrocytes (which may be autologous or allogeneic) chemically coupled with a cocktail containing at least five of twenty immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆), to which T cell responses are demonstrable in early RR-MS patients. Preferred is the use of six, seven, eight or even more (up to 14) of the named immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆).

Even more preferred is the use of one of a cocktail of peptides, wherein the cocktail is selected from:

-   -   a) MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄,         MOG₁₋₂₀ and MOG₃₅₋₅₅     -   b) MBP₁₃₋₃₂, MBP₈₂₋₉₈, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄,         MOG₁₋₂₀ and MOG₃₅₋₅₅     -   c) MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄,         MOG₁₋₂₀, MOG₃₅₋₅₅ and MBP₈₂₋₉₈     -   d) MBP₁₃₋₃₂, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀ and         MOG₃₅₋₅₅.

Further preferred cocktails for use in a method disclosed in this application are cocktails e-oo according to following tables 5.1-5.3. The individual cocktails are disclosed in the columns of said tables. An “X” indicates that the peptide named in the most left column of the table is present in the cocktail. The numbering of the cocktails is provided in the top line of the tables.

TABLE 5.1 Preferred cocktails of peptides e-p for use in the methods disclosed herein: e f g h i j k l m n o p MBP ₁₃₋₃₂ X X X X X X X MBP ₈₃₋₉₉ X X MBP ₈₂₋₉₈ X MBP ₈₂₋₉₉ MBP ₈₂₋₁₀₆ X X X X X X X X X X X MBP ₈₇₋₁₀₆ MBP ₁₃₁₋₁₅₅ X X X X X X MBP ₁₁₁₋₁₂₉ X X X X X X X MBP ₁₄₆₋₁₇₀ X X X X X X X X X PLP ₄₁₋₅₈ X X X PLP ₈₉₋₁₀₆ X X X X PLP ₉₅₋₁₁₆ X X X PLP ₁₃₉₋₁₅₄ X X X X X X X X X PLP₁₇₈₋₁₉₇ X X X X PLP ₁₉₀₋₂₀₉ X X X X X MOG ₁₋₂₀ X X X X X X MOG ₁₁₋₃₀ X MOG ₂₁₋₄₀ X MOG ₃₅₋₅₅ X X X X X X X X X MOG ₆₄₋₈₆ X

TABLE 5.2 Preferred cocktails of peptides q-bb for use in the methods disclosed herein: q r s t u v w x y z aa bb MBP ₁₃₋₃₂ X X X X X X X X X X X MBP ₈₃₋₉₉ X MBP ₈₂₋₉₈ MBP ₈₂₋₉₉ X X MBP ₈₂₋₁₀₆ X X X X X X X X X X MBP ₈₇₋₁₀₆ X MBP ₁₃₁₋₁₅₅ X X X X X X MBP ₁₁₁₋₁₂₉ X X X X X X X X X X MBP ₁₄₆₋₁₇₀ X X X X X X X X X X X PLP ₄₁₋₅₈ X PLP ₈₉₋₁₀₆ X X X X X PLP ₉₅₋₁₁₆ X PLP ₁₃₉₋₁₅₄ X X X X X X X PLP₁₇₈₋₁₉₇ X X X X X PLP₁₉₀₋₂₀₉ X X X X X X X MOG ₁₋₂₀ X X X X X X X MOG ₁₁₋₃₀ X X MOG ₂₁₋₄₀ X X MOG ₃₅₋₅₅ X X X X X X X X X X X X MOG ₆₄₋₈₆ X X

TABLE 5.3 Preferred cocktails of peptides cc-oo for use in the methods disclosed herein: cc dd ee ff gg hh ii jj kk ll mm nn oo MBP ₁₃₋₃₂ X X X X X X X MBP ₈₃₋₉₉ X MBP ₈₂₋₉₈ MBP ₈₂₋₉₉ MBP ₈₂₋₁₀₆ X X MBP ₈₇₋₁₀₆ X X X X X X X X X MBP ₁₃₁₋₁₅₅ X MBP ₁₁₁₋₁₂₉ X X X X X X MBP ₁₄₆₋₁₇₀ X X X X X X X X PLP ₄₁₋₅₈ X X X X PLP ₈₉₋₁₀₆ X X X X PLP ₉₅₋₁₁₆ X X PLP ₁₃₉₋₁₅₄ X X X X X X X X X X X PLP₁₇₈₋₁₉₇ X X X X PLP ₁₉₀₋₂₀₉ X X X X X X X X MOG ₁₋₂₀ X X X X X X X X X X MOG ₁₁₋₃₀ X X MOG ₂₁₋₄₀ X X MOG ₃₅₋₅₅ X X X X X X X X X X X X MOG ₆₄₋₈₆ X X X

In each of the cocktails described herein a MBP peptide may also be replaced with the full length MBP protein. Most preferred of the known MBP proteins is the 18.5 kD isoform (SEQ ID NO: 22). Furthermore any of the MBP peptides may be citrullinated. Moreover, any of the MBP peptides may be replaced with a citrullinated peptide according to SEQ ID NOs: 24-26.

In each of the cocktails described herein a PLP peptide may also be replaced with the full length PLP protein (SEQ ID NO: 21).

In each of the cocktails described herein a MOG peptide may also be replaced with the full length MOG protein (SEQ ID NO: 23).

Most preferred in this aspect of the invention is the use of the cocktail consisting of the following seven peptides MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀ and MOG₃₅₋₅₅.

The preferred route for systemic administration is i.v. administration.

Another preferred aspect of the invention is therefore a therapy based on systemic administration of allogeneic peripheral blood mononuclear cells or red blood cells (erythrocytes) chemically coupled with a cocktail containing at least five of eight immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀, MOG₃₅₋₅₅ and MBP₈₂₋₉₈), to which T cell responses are demonstrable in early RR-MS patients. Preferred is the use of six, seven or eight of the named immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀, MOG₃₅₋₅₅ and MBP₈₂₋₉₈).

Most preferred in this aspect is the use of the cocktail consisting of the following seven peptides MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀ and MOG₃₅₋₅₅.

A still further preferred aspect of the invention is therefore a therapy based on systemic administration of allogeneic peripheral blood mononuclear cells or red blood cells (erythrocytes) chemically coupled with a cocktail containing at least five of twenty immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆), to which T cell responses are demonstrable in early RR-MS patients. Preferred is the use of six, seven, eight or even more (up to 14) of the named immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆).

Most preferred in this aspect is the use of the cocktail consisting of the following seven peptides MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀ and MOG₃₅₋₅₅.

The preferred route for systemic administration is i.v. administration.

Extensive immunological studies, including human in-vitro studies and animal in-vitro and in vivo studies do document the safety, efficacy and in vivo mechanisms of action of the regimens described above.

A few of the many embodiments encompassed by the present description are summarized in the following numbered paragraphs. The numbered paragraphs are self-referential. In this regard, it is explicitly applicant's purpose in setting forth the following paragraphs to describe various aspects and embodiments particularly by the paragraphs taken in combination. That is, the paragraphs are a compact way of setting out and providing explicit written description of all the embodiments that are encompassed by them individually and in combination with one another and, accordingly, applicant specifically reserves the right at any time to claim any subject matter set out in any of the following paragraphs, alone or together with any other subject matter of any one or more other paragraphs, including any combination of any values therein set forth taken alone or in any combination with any other value set forth. Should it be required, applicant specifically reserves the right to set forth all of the combinations herein set forth in full in this application or in any successor applications having benefit of this application.

Aspects of the invention are therefore (amongst others)

-   1.) A blood cell chemically coupled with at least five of the     following eight immunodominant myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀,         MOG₃₅₋₅₅ and MBP₈₂₋₉₈. -   1a) A blood cell chemically coupled with at least five of the     following twenty immunodominant myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆,         MBP₈₇₋₁₀₆) MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆,         PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀,         MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆. -   2) A blood cell chemically coupled with a cocktail containing six,     seven or eight of the following eight immunodominant myelin     peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀,         MOG₃₅₋₅₅ and MBP₈₂₋₉₈. -   2a) A blood cell chemically coupled with a cocktail containing six,     seven, eight or even more (up to 14) of the following twenty     immunodominant myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆,         MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆,         PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀,         MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆. -   3) A blood cell chemically coupled with a cocktail of peptides,     wherein the cocktail is selected from one of the cocktails a-d,     defined above. -   3a) A blood cell chemically coupled with a cocktail of peptides,     wherein the cocktail is selected from one of the cocktails e-oo,     defined above. -   4.) A red blood cell (erythrocyte) chemically coupled with at least     five of the following eight immunodominant myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀,         MOG₃₅₋₅₅ and MBP₈₂₋₉₈. -   4a) A red blood cell (erythrocyte) chemically coupled with at least     five of the following twenty immunodominant myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆,         MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆,         PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀,         MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆. -   5) A red blood cell (erythrocyte) chemically coupled with a cocktail     containing six, seven or eight of the following eight immunodominant     myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀,         MOG₃₅₋₅₅ and MBP₈₂₋₉₈. -   5a) A red blood cell (erythrocyte) chemically coupled with a     cocktail containing six, seven, eight or even more (up to 14) of the     following twenty immunodominant myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆,         MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆,         PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀,         MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆. -   6) A red blood cell chemically coupled with a cocktail a cocktail of     peptides, wherein the cocktail is selected from     -   a) MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄,         MOG₁₋₂₀ and MOG₃₅₋₅₅     -   b) MBP₁₃₋₃₂, MBP₈₂₋₉₈, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄,         MOG₁₋₂₀ and MOG₃₅₋₅₅     -   c) MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄,         MOG₁₋₂₀, MOG₃₅₋₅₅ and MBP₈₂₋₉₈     -   d) MBP₁₃₋₃₂, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀ and         MOG₃₅₋₅₅. -   7.) A peripheral blood mononuclear cell chemically coupled with at     least five of the following eight immunodominant myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀,         MOG₃₅₋₅₅ and MBP₈₂₋₉₈. -   8) A peripheral blood mononuclear cell chemically coupled with a     cocktail containing six, seven or eight of the following eight     immunodominant myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀,         MOG₃₅₋₅₅ and MBP₈₂₋₉₈. -   9) A peripheral blood mononuclear cell chemically coupled with a     cocktail of peptides, wherein the cocktail is selected from selected     from one of the cocktails a-d, defined above. -   9a) A peripheral blood mononuclear cell chemically coupled with a     cocktail of peptides, wherein the cocktail is selected from selected     from one of the cocktails e-oo, defined above.

It has to be understood that in any of the aspects 1-9a described above the blood cells may be autologous or allogeneic in case of red blood cells (erythrocytes). It has to be further understood that in any of the aspects 1-9a described above the blood cells may be autologous in case of peripheral blood mononuclear cells (PBMCs).

BRIEF DESCRIPTION OF THE DRAWINGS

The patent or application filed contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee. Various features and advantages of the embodiments herein described can be fully appreciated as the same becomes better understood when considered in light of the accompanying drawings:

FIG. 1 and FIG. 2 together show results of two separate validation runs on the binding of the peptide to the surface of the cells, as detected by FACS and fluorescence microscopy using fluorophore conjugated streptavidin (Streptavidin-Cy3 and Streptavidin-APC respectively).

In FIG. 1, cells were pulsed in-vitro in the presence or absence of either biotin PLP, EDC or both. The top panel shows cells stained with Streptavidin Cy3. The middle panel shows a plot of streptavidin APC plotted against cell count. The bottom table describes the results of the experiment, in that the peptide on the surface of cells was only detected in the presence of both EDC and biotinPLP.

FIG. 2 shows the biotin peptide is efficiently bound to the cells during the manufacture process in bags. The top panel shows cells stained with Streptavidin Cy3. The middle panel shows a plot of streptavidin APC plotted against cell count. The open histogram shows PBMC after lysis, before the coupling reaction; the filled histogram shows the product (PBMC after coupling reaction).

FIG. 3 shows that presence of peptide-coupled cells did not induce proliferation in PBMC compared to unstimulated PBMC or PHA stimulated PBMC. The inset shows counts with PBMC treated with EDC but without peptide (tAPC), prep (tAPCprep) or without further stimulus (APC).

FIG. 4 shows that there is no significant induction of various inflammatory cytokines (e.g., IL10, IFNγ, IL10, IL1 §, TNFα) at 3 hr and 24 hr in the presence of peptide-coupled PBMC compared to the negative control (APC).

FIG. 5 shows the concentrations of cytokines (at 3 hr and 24 hr) without PHA control.

FIG. 6 shows cytokine response in PBMC pre-activated with PHA and cultured in the presence of APC, tAPC or tAPCpep. It can be seen that there was no induction of proliferation in response to peptide-coupled cells.

FIG. 7 shows a plot of cytokine release (at 3 hr and 24 hr) in response to peptide-coupled cells.

FIG. 8 shows proliferative response of the TCC, as measured by ³H-Thymidine incorporation after 72 h.

FIG. 9 shows that proliferation of the TCC can be recuperated by the addition of either IL-2 or the anti-CD28 antibody in the presence of peptide-coupled cells.

In an animal model of MS, experimental autoimmune encephalomyelitis (EAE), this protocol has shown dramatic therapeutic efficacy on clinical and pathological signs of disease. It not only silences the immune response against the major autoantigen, but also prevents epitope spreading to other myelin peptides within the same protein (intramolecularly) and also additional myelin proteins (intermolecularly), which represents an important advantage over other therapies. It is expected that treatment will decrease the average number of monthly contrast-enhancing MRI lesions by 50% or greater and reduce the number, change the phenotype of myelin peptide-specific T cells from a pro-inflammatory Th1/Th17 to an anti-inflammatory Th2-like type and/or render autoreactive T cells anergic.

Advantages of the protocol are: 1. Tolerance is exquisitely antigen-specific and therefore will not alter the normal immune response as do current immunosuppressive regimens. 2. From preclinical studies it was noted that in most cases a single intravenous infusion of peptide-pulsed peripheral blood mononuclear cells (PBMC) will induce long-term amelioration, which is a substantial improvement compared to all current therapies.

If needed, patients may be treated more than once in their life-time (they may be re-treated as needed e.g. on a yearly basis). 3. Tolerance is inducible in both naïve and activated Th1 cells. It is considered safer and more effective than tolerance induced by peripheral administration of soluble peptide or DNA vaccination with myelin peptide, which are both currently in phase II and -III clinical testing.

MS and Role of T Cells:

Current evidence suggests CD4+ autoreactive T cells as a central factor for the autoimmune pathogenesis of MS probably relevant not only for the induction and maintenance of the autoimmune response, but also during tissue damage (Sospedra and Martin 2005, Annu. Rev. Immunol. 23:683). The frequency of activated CD4+ T cells reactive to main constituents of the myelin sheath, such as myelin basic protein (MBP), proteolipid protein (PLP) and myelin oligodendrocyte glycoprotein (MOG) is increased in MS patients. The instant application further demonstrates that high avidity myelin-specific T cells, which derive from the memory T cell pool and preferentially express a Th1 cytokine phenotype, are clearly more frequent in MS patients than in controls (Bielekova et al. 2004, J. Immunol. 172:3893). Due to their pathogenetic involvement CD4+ T cells are one logical target for therapeutic interventions. Tolerization by peptide-pulsed, fixed APC in the animal model of MS: Many pathological characteristics of human MS are reflected in the situation of EAE, a paradigmatic model of Th1/Th17 cell-driven autoimmune disease. Studies in relapsing EAE (R-EAE) in the SJL mouse have clearly shown that chronic demyelination involves the activation of T cell responses to multiple endogenous antigens arising via epitope spreading (Vanderlugt and Miller 2002, Nat. Rev. Immunol 2:85). Unresponsiveness of T cells can be induced when antigen presenting cells (APC) pulsed with antigenic peptide are treated with the cross linker 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (ECDI, sometimes also referred to as EDC).

A still further aspect of the invention is a peripheral blood mononuclear cell as described above in which the chemical coupling is achieved by 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (ECDI) which is preferred over other possible coupling agents.

Preclinical experiments have proven that a single i.v. injection of naïve murine splenocytes pulsed with a mixture of encephalitogenic myelin peptides and fixed with the cross linker ECDI is highly efficient in inducing peptide-specific tolerance in vivo. In EAE this protocol not only prevented animals from disease but even effectively reduced the onset and severity of all subsequent relapses when given after disease induction, indicating that specific tolerance can down regulate an ongoing autoimmune response (Kohm and Miller 2005, Int. Rev. Immunol. 24:361). More relevant to the treatment of MS, studies in EAE have shown that tolerance can be simultaneously induced to multiple epitopes using a cocktail of encephalitogenic myelin peptides, thus providing the capacity to target autoreactive T cells with multiple specifities. This regimen of antigen-specific peripheral tolerance is superior to tolerance induction by oral, subcutaneous or intraperitoneal administration of antigen and has also proven to be safe and effective in other experimental models of different T cell driven autoimmune diseases and in allograft rejection. Tolerization of human T cells by autologous antigen-coupled APCs treated with ECDI is effective in vitro as shown by failure of tolerized T cells to proliferate or to produce Th1 cytokines and a decreased expression of costimulatory molecules on these cells (Vandenbark et al. 2000, Int. Immunol. 12:57). There is evidence that at least two distinct mechanisms are involved in the induction of antigen specific tolerance by this regime. 1) Direct tolerance where Th1 clones encountering nominal antigen/MHC complexes on chemically-fixed APCs were anergized as a result of failure to receive adequate CD28-mediated costimulation (Jenkins and Schwartz. 1987, J. Exp. Med. 165:302) and 2) an indirect mechanism (cross tolerance) where tolerance is induced by reprocessing and re-presentation of antigens by host APCs (Turley and Miller, 2007, J. Immunol 178:2212). Treatment of cells with ECDI induces apoptosis in a substantial percentage of treated cells. Thus an indirect mechanism that involves fixed APC undergoing apoptosis, which are then processed and represented by host APC, is likely. This is further supported by effective induction of tolerance in MHC deficient and allogeneic mice. In-vitro bone marrow derived dendritic cells effectively phagocyte and process antigen pulsed, fixed APC. Choice of Peptides for Tolerization: Based on the rationale that T cells that recognize myelin peptides with high functional avidity might be most relevant for the autoimmune process in MS, embodiments of the present application provide high avidity myelin-specific T cells and employed 20 myelin peptides derived from MBP, PLP and MOG (Bielekova et al. 2004, J. Immunol. 172:3893). In summary these studies showed the following: (1) high avidity myelin-specific T cells are clearly more frequent in MS patients than in controls; (2) most of these T cells are derived from the memory T cell pool, and (3) express a Th1 cytokine phenotype; (4) only myelin epitopes MBP₁₃₋₃₂, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀ and MOG₃₅₋₅₅ contributed to the increased reactivity observed in MS patients and (5) each those peptides against which high avidity T cells are mainly directed, is predicted as a poor binder to the main MS-associated HLA-DR alleles, which indicates that myelin peptides that bind poorly to MS-associated DR alleles are less likely to induce negative selection in the thymus. It should be noted that MBP peptide₈₃₋₉₉ will be included because this peptide has been shown to be immunodominant in MS patients by many prior studies.

Antigen-Coupled Cell Tolerance in Humans—the ETIMS Approach

A first-in-man trial (ETIMS trial) was conducted in MS patients with the aim to assess the feasibility, safety and tolerability of this novel tolerization regimen, which employs a single infusion of autologous peripheral blood mononuclear cells chemically coupled with seven myelin peptides (MOG₁₋₂₀, MOG₃₅₋₅₅, MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀ and PLP₁₃₉₋₁₅₄). In the open-label, single center, dose escalation study, nine MS patients (7 relapsing-remitting and 2 secondary progressive; EDSS 1-5.5), who were off-treatment for standard therapies were treated with a single infusion of ETIMS product. All patients had to show T cell reactivity against at least one of the myelin peptides used in the trial. Neurological, MRI, laboratory and immunological examinations were performed to assess the safety, tolerability and in vivo mechanisms of action of this regimen. Overall, administration of antigen-coupled cells was feasible, had a favorable safety profile and was well tolerated in MS patients. Compared to the pre-treatment observation period there was no increase in clinical and MRI parameters of disease activity by this regimen. Patients receiving the high dose (>1×10⁹) of peptide-coupled cells showed a decrease in antigen-specific T cell responses following ETIMS therapy (Lutterotti et al. 2013).

Further aspects of the invention therefore include:

-   10) A pharmaceutical composition containing blood cells as described     herein for systemic administration. -   11) A pharmaceutical composition containing blood cells as described     herein for i.v. administration. -   12) A medical product containing at least one cell as described     herein. -   13) The use of cells as described herein for the manufacture of a     medicament for the treatment of MS. -   14.) The use of cells as described herein for the manufacture of a     medicament for the treatment of MS, characterized in that the cells     are allogeneic cells. -   15) The use of cells as described herein for the manufacture of a     medicament for the treatment of MS, characterized in that the cells     are autologous cells. -   16) A method of treating patients suffering from MS by systemic     administration of a pharmaceutical composition containing blood     cells coupled with a cocktail of peptides as described herein.

ETIMS is a cell-based tolerization therapy that involves autologous antigen-presenting cells pulsed with a specific set of myelin peptides in the presence of a chemical coupling agent. This therapy is in many aspects novel and unique. These include a) the use of a set of peptides that covers the immunodominant epitopes of those myelin proteins, which are targeted by the high-avidity autoimmune T cell response in MS, b) different from all other tolerization therapies, ETIMS was shown to prevent epitope spreading, i.e. the broadening of the autoimmune response to other target epitopes, c) based on extensive animal testing, ETIMS is expected to be safer and more effective than those tolerization therapies that are currently in clinical testing in MS, i.e. administration of a single soluble peptide intravenously by BioMS and intramuscular administration of a plasmid encoding a myelin peptide together with a Th2 cytokine by Bayhill Pharmaceuticals, d) it was contemplated that only a single treatment is required, which represents a major advantage with respect to patient acceptance.

The specificity, lack of side effects, and single time administration are considered major advantages of this treatment.

The scientific strategy follows two major goals: 1. To establish the efficacy and safety of ETIMS as a tolerizing treatment in early MS, and 2. To establish the precise in vivo mechanism of action of ETIMS. These mechanistic studies will include the exploration of more selective cell populations for tolerization, e.g. immature dendritic cells, B cells, others, in order to improve both efficacy and our intellectual property position.

Ideally peptide specific immune tolerance should be achieved early in the inflammatory phase of the disease, where blockade of the autoreactive immune response can inhibit dissemination and propagation of the disease and irreversible disability can be prevented. Therefore the targeted patient group are relapsing-remitting MS patients early in the disease course or even patients presenting with a first clinical event suggestive of MS, i.e. clinically isolated syndromes (CIS). At this time point MS patients generally have a low grade of neurologic disability, which allows them to participate in all activities of daily life and work without significant compromise.

One further aspect of the invention is a medicinal product for human use (ETIMS) containing blood cells that have been pulsed with at least five of eight immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀, MOG₃₅₋₅₅ and MBP₈₂₋₉₈) and fixed with the cross-linker ECDI. Preferred blood cells are red blood cells, more preferred blood cells are peripheral blood mononuclear cells (PBMC). The blood cells may be autologous or allogeneic.

Another further aspect of the invention is a medicinal product for human use (ETIMS) containing blood cells that have been pulsed with at least five of twenty immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆) and fixed with the cross-linker ECDI. Preferred blood cells are red blood cells, more preferred blood cells are peripheral blood mononuclear cells (PBMC). The blood cells may be autologous or allogeneic.

A preferred aspect of the invention is a medicinal product for human use (ETIMS) containing blood cells that have been pulsed with six, seven or eight of eight immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀, MOG₃₅₋₅₅ and MBP₈₂₋₉₈) and fixed with the cross-linker ECDI. Preferred blood cells are red blood cells, more preferred blood cells are peripheral blood mononuclear cells (PBMC). The blood cells may be autologous or allogeneic.

A further preferred aspect of the invention is a medicinal product for human use (ETIMS) containing blood cells that have been pulsed with six, seven, eight or even more (up to 14) of twenty immunodominant myelin peptides (MBP₁₃₋₃₂, MBP₈₃₋₀₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆) and fixed with the cross-linker ECDI. Preferred blood cells are red blood cells, more preferred blood cells are peripheral blood mononuclear cells (PBMC). The blood cells may be autologous or allogeneic.

An even more preferred aspect of the invention is a medicinal product for human use (ETIMS) containing blood cells that have been pulsed with a cocktail of peptides according to the foregoing and the following aspects, wherein the cocktail is selected from one of the cocktails a-d or e-oo, defined above, and fixed with the cross-linker ECDI. Preferred blood cells are red blood cells (erythrocytes), more preferred blood cells are peripheral blood mononuclear cells (PBMC). The blood cells may be autologous or allogeneic.

The safety, preliminary efficacy and in vivo mechanisms of action of ETIMS in early relapsing remitting MS patients can be demonstrated in a clinical trial.

Manufacture Process:

The manufacturing process for the blood cells according to the invention is described below by way of example. It has to be understood that this description is not limiting in any way. An expert in the art is able to adapt the example to specific needs without any need to be inventive. The description below is in particular easily adaptable to other types of blood cells.

The excipients erythrocyte lysis buffer and peptide solution may be produced in advance and stored at <−20° C.

Peptide Solution

The peptide solution is prepared in the clean room (Category A) in the Department of Transfusion Medicine. First, 30 (±3) mg of each single peptide are weighed in and solved in 7.5 ml of water for injections (final concentration of peptide 4 mg/ml), respectively. Thereafter all peptides are pooled by transferring 5 ml of each single-peptide solution into a new tube and adding 5 ml of water for injections (total volume 40 ml) to obtain a final concentration of 0.5 mg/ml of each single peptide. Peptide-pool solution may be aliquoted in 1.5 ml aliquots (20 aliquots) in sterile and endotoxin free NUNC Cryo Tube vials (NalgeNunc International) and stored at −20° C. until use or may be used directly in the manufacturing process. 5 ml of the Peptide-pool solution are transferred into a blood-bag containing 30 ml of water for injections for sterility testing. 5 ml are aliquoted at 1 ml and stored at −20° C. for later quality controls. Frozen peptide-pool solutions have to pass sterility control before they can be used in the manufacture process. The identity and presence of each single peptide in the pool may be verified. The maximum storage time is 3 months.

At the day of manufacture of drug product, 1 ml of peptide-solution is transferred to a blood bag (P1459, Fresenius; see IMPD 2.1.P.3.5 Filling of blood bags in clean room). The procedure is done in the clean room (category A). The blood bag containing the peptide solution is stored at 4° C. until use.

Erythrocyte Lysis Buffer

The preparation of the erythrocyte lysis buffer is done in the clean room. Briefly, 4 g of Ammonium chloride EMPROVE® Ph Eur and 0.5 g of Potassium hydrogen carbonate EMPROVE® Ph Eur are solved in 50 ml of water for injection (Ph Eur). Using a 50 ml syringe 25 ml of the solved lysing buffer are transferred to a blood bag through a sterile filter (0.2 μm, Millipore). The blood bag is filled up to 200 ml with water for injection and stored at −20° C. until use. Two bags are filled. 50 ml of lysis buffer are transferred to a blood bag for sterility testing and 50 ml are preserved at −20° C. for later quality control. Erythrocyte lysis buffer solutions have to pass sterility control before they can be used in the manufacture process. The maximum storage time is three months.

CPD/Saline Washing Solution

At the day of the manufacture process a CPD bag (Compoflex, Fresenius) containing 63 ml of CPD will be filled up to 500 ml with sterile physiologic saline (NaCl 0.9%, Baxter) solution. Bags will be connected by TSCD. A balance (PC4000, Mettler) is used to control for weight (500 g). Two bags are produced. At the end of the manufacture process residual washing solution is tested for sterility.

EDC Solution

In the clean room (Cat. A) 200 mg EDC are solved in 2 ml of water for injection. Using a sterile syringe 1 ml is transferred to a blood bag (P1459, Fresenius). The blood bag with the EDC solution is stored at 4° C. until use. Residual EDC is tested for sterility.

Collection of PBMC and Plasma

At the day of blood collection 2.5-5×10⁹ PBMC will be isolated from study-qualifying MS patients by standard leukapheresis, performed according to policies and procedures at the Department of Transfusion Medicine. For the collection of cells, a standardized automatic program (AutoPBSC) on a Cobe Spectra apheresis machine (Cobe Spectra) was used. The AutoPBSC processes 4500 ml of blood and enriches PBMC in 6 harvest phases with approximately 10 ml volume each. In parallel to the collection of cells, 120 ml of autologous plasma will be collected during the apheresis procedure and stored at 4° C. in a standard blood bag. During the whole apheresis procedure ACD-A (Baxter) is used as anticoagulant to prevent clotting of blood. The AutoPBSC program uses ACD-A at 0.083 ml/ml (relation 1:12), however the amount can be adapted within defined ranges (0.071-0.1 ml/ml), if necessary. At the end of the apheresis the concentration of ACD-A in the cell product and plasma is documented in the production log.

Cell Processing

All steps described here are done maintaining a closed system. In practice excipients are pre-filled in blood bags in the clean room (category A) and added to the cells by connecting the bags using a sterile tubing welder (TSCD®, Terumo). The apheresate is transferred to a standard blood bag (Compoflex P1461 500 ml, Fresenius) by welding the tubes of the bags with the TSCD®. A small retention sample is maintained in the original blood bag that will be used for counting of cells after bags have been separated using a portable tubing sealer (Fresenius NBPI). Next, cells are separated from plasma by centrifugation at 300×g for 15 min at room temperature (RT). Plasma is removed from the bag by pressing it to a sterile connected empty bag, using a plasma extractor (Baxter). The bags are separated by a portable tubing sealer. To lyse erythrocytes the bag containing the erythrocyte lysing buffer (ACK) is connected by the TSCD and the cell pellet is resuspended in 200 ml erythrocyte lysis buffer and incubated for 15 min, RT, shaking (3 rpm) on a wave platform shaker (Heidolph). At the end of the incubation period cells are washed with 200 ml CPD 12.6%/saline and centrifuged for 15 min at 200 g at 4° C. Supernatant is removed from the bag by pressing it to an empty bag, using a plasma extractor. The cells are washed again with 200 ml CPD 12.6%/saline. Cells are centrifuged for 15 min at 200 g at 4° C. and supernatant is removed from the bag. Cells are transferred to a 150 ml bag (Compoflex 1459, Fresenius) and a retention sample is taken for cell counting. 1.5-7×10⁹ PBMC will be re-suspended in 20 ml saline and 1 ml peptide-pool solution containing 0.5 mg/ml of each GMP manufactured peptide added. The selected peptides (e.g. MBP1, MBP2, MBP3, MBP4, PLP1, MOG1 and MOG2) will be used for coupling. The coupling reaction is initiated by the addition of 1 ml of 100 mg/ml of freshly prepared water-soluble 1-ethyl-3-(3-dimethylaminopropyl-)-carbodiimide (EDC). Following 1 h incubation shaking at 4° C., the peptide-coupled cells are washed 2 times with 100 ml CPD/saline and finally re-suspended in autologous plasma at a concentration given by the specification (1×10⁶, 1×10⁶ or 1×10⁷ cells/ml). At this time sample is taken for release testing prior to infusion. Cells will be carefully checked for the absence of clumping. 100 ml of final ETIMS cell product will be infused using a standard blood transfusion kit with inline-filter (200 μm). The control of critical steps and intermediates are described in IMPD 2.2.P.3.4 and the flow chart (IMPD Figures 2.1.P.3.3 1-3).

The whole manufacture process is performed within standard blood bags in a functionally closed system. In practice peptides, lysis buffer and washing solutions are filled in standard blood bags under sterile and endotoxin free conditions in a licensed clean room laboratory (category A, ISO14644 certified)) following strict GMP standards at Department of Transfusion Medicine. In the manufacture process the addition of these materials/reagents are carried out by welding the tubes of the respective blood bags with a sterile tubing welder (Terumo TSCD®).

The most preferred coupling agent for the process described above is by 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (ECDI) as described above. However, other coupling agents (e.g. based on different carbodiimides) do qualify as well.

Further aspect of the invention therefore are:

-   17) A process for the manufacture of a peripheral blood mononuclear     coupled with at least five of the following eight immunodominant     myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀,         MOG₃₅₋₅₅ and MBP₈₂₋₉₈,     -   containing the steps of isolating peripheral blood mononuclear         cells, adding the selected peptides and subsequent adding of the         coupling agent. -   17a) A process for the manufacture of a peripheral blood mononuclear     coupled with at least five of the following twenty immunodominant     myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆,         MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆,         PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀,         MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆,     -   containing the steps of isolating peripheral blood mononuclear         cells, adding the selected peptides and subsequent adding of the         coupling agent. -   18) A process for the manufacture of a peripheral blood mononuclear     coupled with six or seven or eight of the following eight     immunodominant myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀,         MOG₃₅₋₅₅ and MBP₈₂₋₉₈,     -   containing the steps of isolating peripheral blood mononuclear         cells, adding the selected peptides and subsequent adding of the         coupling agent. -   18a) A process for the manufacture of a peripheral blood mononuclear     coupled with six or seven, eight or even more (up to 14) of the     following eight immunodominant myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆,         MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆,         PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀,         MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆,     -   containing the steps of isolating peripheral blood mononuclear         cells, adding the selected peptides and subsequent adding of the         coupling agent. -   19) A process for the manufacture of a peripheral blood mononuclear     coupled with at least five of the following eight immunodominant     myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀,         MOG₃₅₋₅₅ and MBP₈₂₋₉₈,     -   in which the coupling agent is ECDI. -   19a) A process for the manufacture of a peripheral blood mononuclear     coupled with at least five of the following eight immunodominant     myelin peptides:     -   MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆,         MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆,         PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀,         MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆,     -   in which the coupling agent is ECDI.

It has to be understood that in any of the aspects 17-19 described above the blood cells may be autologous or allogeneic.

Validation of the Manufacture Process Validation of Infrastructure and Technical Equipment

Several validation runs arte to be performed to assure that the infrastructure and the technical equipment are suitable for the manufacture process. The collection of cells will be performed in a apheresis unit such as the Department for Transfusion Medicine, UKE (see also Validation of leukapheresis) following SOPs. Cells will be processed in a Clean room. Washing, centrifugation and incubation steps will be done in a clean room Category D (Room 29) while maintaining a closed system. The system will be opened only in the clean room category A. All procedures will be performed by trained personnel only.

All technical equipment used for the processing of cells is certified for its intended use and maintained following SOP's. Only material that has passed the Quality control will be used.

Validation of Leukapheresis

Validation of the apheresis protocol and the characterisation of the cell product were done with aphereses from healthy donors and MS patients. All Aphereses were run on a CobeSpectra apheresis machine at the Department for Transfusion Medicine, UKE. The AutoPBSC program has been selected for several reasons (Table 1). 1) By processing a standardized blood volume (4500 ml), a sufficient yield of cells was obtained. 2) The cell product has a high purity of mononuclear cells in a standardized volume of the cell product. 3) Compared to the manual program the erythrocyte count is lower.

TABLE 1 Blood Volume Product % % ApheresisDuration (ml) of Volume PBMC × lymphocytes monocytess (min) patient (ml) 10⁹ (within MNC) (within MNC) 290SA 128 4500 61 5.5 77.6 17.8 IJ1804  86 4552 61 5.1 80.2 13.4 445CO  88 3908 61 5.5 67.7 15.2 978TH  99 5502 61 5.5 62.4 21.5 RM1401 102 5153 60 4.2 71.0 22.8 IJ2801 115 5747 60 2.7 82.6 10.8 1066ST 112 3479 61 5.5 72.9 16.7

Validation of Erythrocyte Lysis

Although the apheresis product contains a very low number of erythrocytes, in absolute numbers erythrocytes outweigh mononuclear cells 10 to 40 times. Thus it is necessary to lyse erythrocytes to obtain a higher purity of the cell product. For the lysis of erythrocytes an established lysis buffer (ACK-buffer) was used. The efficiency of the lysis buffer in buffy coats, which contain a much higher amount of erythrocytes compared to apheresate, was tested. In buffy coat, efficient lysis of erythrocytes (mean hemoglobin (Hb) before lysis 10.03 g/dl, after lysis 0.63 g/dl; Table 2) was achieved. In aphereses the content of erythrocytes is much lower from the beginning and is below measurable values after lysis.

TABLE 2 Hb before lysis Hb after lysis Product (g/dl) (g/dl) BC9198169 8.4 0.4 BC9204876 12.6 1.0 BC9247719 9.8 0.5 BC9261124 9.32 0.6

Filling of Blood Bags in Clean Room

All reagents will be filled through a sterile tube which has a Luer-lock device. The tube will be welded to the bag using a sterile welding device. After the reagents have been filled in the bag, the tube will be separated using a portable tubing sealer.

Cell Number

The absolute cell number in the product is a critical point in the manufacture process. During the manufacture process cells are lost (Table 3). Thus it is essential to define minimal cell numbers that are required for the production of the ETIMS product. These cell numbers have to be checked through in-process controls. The acceptance criteria for the cell numbers necessary for the manufacture process have been defined in several validation runs using buffy coats. The cell content of buffy coat is approximately 1×10⁹ cells, thus for the validation runs a final cell number of 5×10⁸ cells was targeted. Cell counts were assessed before starting the manufacture process, before the coupling reaction and after the last washing step. In all validation runs the target cell count could be reached, when the initial cell number was higher than 1.2×10⁹.

TABLE 3 Duration Initial Cell count after Cell count after Buffy coat (min) Cell count lysis coupling 9261124 320 16.5 × 10⁸   9.95 × 10⁸ 7.2 × 10⁸ 9247719 330 17 × 10⁸   11 × 10⁸ 6.5 × 10⁸ 9204876 380 15 × 10⁸ 11.4 × 10⁸  10 × 10⁸ 9198169 350 12 × 10⁸  8.6 × 10⁸  11 × 10⁸

Duration of Manufacture Process

An aim was to reduce the duration of the manufacture process in order to enhance viability and lower the risk of microbiological contamination. Since in several validation runs residual amounts of EDC could not be detected in the first washing solution after the coupling reaction, a washing step after the lysis of erythrocytes and one after the coupling reaction was reduced. This led to a reduction of the manufacture process of approximately 57 minutes. The reduction of the duration of the manufacture process was paralleled by an increase in cell viability measured as membrane integrity by FACS-Analysis (Ph Eur 2.7.29). The mean duration is 292 min (Table 4).

TABLE 4 Duration Initial Cell count after Cell count after Product (min) Cell count lysis coupling RM1401 295   2 × 10⁹ 1.4 × 10⁹ 1.2 × 10⁹ IJ2801 295 2.5 × 10⁹ 2.2 × 10⁹ 1.8 × 10⁹ 9373085 285 1.3 × 10⁹ 1.0 × 10⁹ 0.8 × 10⁹ pH

The mean pH in the product after resuspension in human plasma was pH 7.7 (range 7.6-7.8; n=8). Autologous plasma was used in validation runs with apheresate and third party plasma matched for blood group in validation runs with buffy coat. pH was measured in supernatants of washing steps. The pH of lysis buffer is pH 7.4 the pH of the CPD buffer is pH 5.8.

Viability

Cell viability was assessed by measuring membrane integrity by Trypan blue exclusion and FACS (Ph.Eur. 2.7.29) at different time-points and storage conditions. (see IMPD 2.1.P.8).

Peptide Binding

An objective of the study was to evaluate whether efficient coupling of peptides to the surface of PBMC could be achieved in the manufacture process in bags.

In-vitro it was demonstrated that the presence of both EDC and peptide is necessary for efficient binding of peptide to the cell surface (Figure 2.1.P.3.5-1).

To assess the efficiency of the coupling reaction in the manufacture process in bags, one of the seven peptides (PLP₁₃₉₋₁₅₄) has been replaced by a biotinylated peptide (biotinPLP₁₃₉₋₁₅₄). Binding of the peptide to the surface of the cells has been detected by FACS and fluorescence microscopy using fluorophore conjugated streptavidin (Streptavidin-Cy3 and Streptavidin-APC respectively). In the present study, using two separate validation runs, it was demonstrated that the peptide is binding efficiently to the surface of PBMC during the manufacture process in bags. One result representative of 2 independent validation runs is for example shown in FIG. 1.

Since the volume for the coupling reaction might vary (target volume 10 ml), the efficiency of the coupling procedure was assessed in 4 different volumes. At a concentration ranging for PBMC: 1×10⁷-0.33×10⁷ cells/ml; for EDC: 100 mg/ml-33 mg/ml and for peptide-pool at 0.05 mg/ml-0.017 mg/ml peptide the binding is efficient. Further reduction of the concentration reduces the binding efficiency below accepted levels. Thus a volume range of 10-20 ml for the coupling procedure is acceptable.

Sterility

Sterility was maintained in 5 independent validation runs. Samples were tested for aerobial and anaerobial bacteria and fungi.

Endotoxin

Final washing solutions of 3 validation runs were tested for the presence of endotoxins (Pyrogene®, Lonza). Endotoxin (<0.5 EU/ml) could not be detected in the supernatant of the last washing solution before resuspension of cells in autologous plasma. The presence of endotoxins cannot be assessed in human plasma, since plasma inhibits the test.

Aggregates

Several measures were taken to ensure against the presence of aggregates.

-   a) Aggregates were not observed by visual inspection in any of the     products in the validation runs (n=14). The infusion on the bench     was stimulated with the blood transfusion kit with an inline filter     (200 μm) that will be used for patients. Aggregates were not     observed in the filter after having passed the cells. To further     ensure against aggregates, the cell concentration was counted before     and after having passed through the filter and yet no differences     were observed (n=2). -   b) The presence of aggregates was assessed by microscopy in a blood     smear or after transferring cells to a cell culture plate. No     differences were observed in the cells compared to non-treated     cells. -   c) In order to detect and quantify micro-aggregates several products     (n=5) were analyzed by FACS. Measurement of the forward scatter area     (FSC-A) and the forward scatter width (FSC-W) did not reveal a     higher frequency of micro-aggregates in the cell product compared to     the cells before EDC treatment. The frequency of aggregates did not     increase during the storage period of 4 h. -   d) Injection of human product (ETIMS) in mice (n=20) did not lead to     embolism, because of aggregates in any of the mice.

Identity

The cellular composition of the apheresate and the final drug product was analyzed with the objective to evaluate differences in the final cellular composition of the drug product resulting from the processing of the cells. A clear phenotypic characterisation of the final product is hampered by the treatment of the cells, most probably because the chemical treatment alters the target structure for the specific antibodies. Thus, the cell product ias to be phenotyped before the processing of the cells in order to assess whether the relation between different populations (T cells, B cells, monocytes) have an influence on the treatment outcome. The aim is to establish acceptance criteria for the further development of the drug product.

Pre-Clinical Safety

Animal Studies:

Two different experimental settings were used for the assessment of toxicity. 1) Toxicologic testing of the human product can only be assessed in the short term because of immunotoxicity when tested in different species. Thus the short term toxicity of the human product was assessed in immune-compromised mice (severe combined immunodeficiency; SCID). 2) Mid-term toxicity of syngeneic splenocytes coupled with the seven myelin peptides used in the trial was assessed in the SJL model.

Both toxicological studies were conducted by LPT Laboratory of Pharmacology and Toxicology GmbH & Co. KG, Redderweg, Hamburg, a GLP-certified laboratory.

Acute Toxicity Study of Human Peptide-Coupled Peripheral Blood Mononuclear Cells (PBMC) and Human Plasma by Single Intravenous Administration to SCID Mice (LPT 22043).

Test item 1 × 10⁹ Human PBMC chemically coupled to seven myelin peptides (MBP₁₃₋₃₂ (MBP1), MBP₈₃₋₉₉ (MBP2), MBP₁₁₁₋₁₂₉ (MBP3), MBP₁₄₆₋₁₇₀ (MBP4), MOG₁₋₂₀ (MOG1), MOG₃₅₋₅₅ (MOG2), PLP₁₃₉₋₁₅₄ (PLP1)) resuspended in 100 ml human plasma. Human plasma served as control Number of experiments Two different, at two independent time-points, manufactured human peptide-coupled PBMC (Product A and Product B) Number of animals per 5 males and 5 females received peptide-coupled experiment cells, 1 male and 1 female received human plasma as control Intravenous injection Dose/approx. 15 seconds Administration volume 200 μl i.v. Dose 2 × 10⁶ peptide-coupled human PBMC Body weight (at start of treatment) Males: 17-22 g Females: 15-17 g Age (at start of treatment) Males: 41-48 days Females: 41-48 days Identification of animal By coloured marks and cage label Duration of experiment At least 5 adaptation days 1 test day 24 hours recovery period Evaluation Observations were performed for all animals and recorded systematically (with individual records being maintained for each animal) before and immediately, 5, 15, 30 and 60 min, as well as 3, 6 and 24 hours after administration. Observation Changes of skin and fur, eyes and mucous membranes, respiratory and circulatory function, autonomic and central nervous system and somatomotor activity as well as behaviour pattern were observed. Attention was also paid to possible tremor, convulsions, salivation, diarrhoea, lethargy, sleep and coma. Observations on mortality were made with appropriate actions taken to minimize loss of animals during the study. Measurements Individual body weights were recorded before administration of the test item and after 24 hours. Changes in weight were calculated and recorded. At the end of the experiments all animals were sacrificed under ether anaesthesesia by cutting the aorta abdominalis, exsanguinated, weighed, dissected and inspected macroscopically under the direction of a pathologist.

Summarized Results

Under the present test conditions, single intravenous injections of 200 μL Human peptide-coupled peripheral PBMC (Product A), human peptide-coupled PBMC (Product B) or human plasma to mice did not lead to any signs of toxicity. No mortality occurred.

Product A Product B Human Plasma Symptoms/Criteria males females males females males females Clinical signs none none none none none none mortality within 6 h 0 0 0 0 0 0 within 24 h 0 0 0 0 0 0 Mean body weight start 18.6 15.6 20.4 16.2 20.5 17.0 after 24 h 19.0 15.8 20.6 16.4 20.5 17.5 Inhibition of body none none none none none none weight gain Necropsy findings * none 2 of 5 4 of 5 4 of 5 2 of 2 2 of 2 * A reduced spleen size was observed in 0 of 5 male and 2 of 5 female animals treated with Product A, 4 of 5 male and 4 of 5 female animals treated with Product B and 2 of 2 male and 2 of 2 female animals treated with human plasma.

Acute Toxicity Study of Peptide Coupled Splenocytes by Single Intravenous Administration to SJL Mice (LPT 21988)

Test item Syngeneic splenocytes chemically coupled to seven myelin peptides (MBP₁₃₋₃₂ (MBP1), MBP₈₃₋₉₉ (MBP2), MBP₁₁₁₋₁₂₉ (MBP3), MBP₁₄₆₋₁₇₀ (MBP4), MOG₁₋₂₀ (MOG1), MOG₃₅₋₅₅ (MOG2), PLP₁₃₉₋₁₅₄ (PLP1)) resuspended in PBS. Number of experiments 1 Number of animals per 5 males and 5 females received peptide-coupled splenocytes experiment Intravenous injection Dose/approx. 15 seconds Administration volume 200 μl iv. Dose 5 × 10⁷ peptide-coupled splenocytes Body weight (at start of treatment) Males: 17-19 g Females: 17-18 g Age (at start of treatment) Males: 43 days Females: 43 days Identification of animal By coloured marks and cage label Duration of experiment At least 5 adaptation days 1 test day 2 recovery weeks Evaluation Observations were performed for all animals and recorded systematically (with individual records being maintained for each animal) before and immediately, 5, 15, 30 and 60 min, as well as 3, 6 and 24 hours after administration. All animals were observed for a period of 14 days. Observation Changes of skin and fur, eyes and mucous membranes, respiratory and circulatory function. autonomic and central nervous system and somatomotor activity as well as behaviour pattern were observed. Attention was also paid to possible tremor. convulsions, salivation. diarrhoea, lethargy, sleep and coma. Observations on mortality were made at least once daily with appropriate actions taken to minimize loss of animals during the study. Measurements Individual body weights were recorded before administration of the test item and thereafter every day for the first three days followed by weekly intervals up to the end of the study. Changes in weight were calculated and recorded. At the end of the experiments all animals were sacrificed under ether anaesthesesia by cutting the aorta abdominalis, exsanguinated, weighed, dissected and inspected macroscopically under the direction of a pathologist.

Summarized Results

Under the present test conditions, a single intravenous injection of 5×10⁷ peptide-coupled splenocytes to mice did not lead to any signs of toxicity. No mortality occurred. All animals gained the expected body weight throughout the whole study period.

5 × 10⁷ cells/ animal iv. n = 5 Symptoms/Criteria males females Clinical signs none none mortality within 6 h 0 0 within 24 h 0 0 within 7 d 0 0 within 14 d 0 0 Mean body weight start 18.2 17.6 after 7 d 19.8 18.4 (+8.8) (+29.2) after 14 d 22.4 20.6 (+23.1) (+37.8) Inhibition of body weight none none gain Necropsy findings none none D = days H = hours In brackets: body weight gain in %, compared with the start value i.v. = intravenous

In-Vitro Analysis with Human Cells:

The treatment is only administered once to patients and is being administered by the tolerogenic i.v. route with cells undergoing apoptosis. Thus there is little concern that a cytotoxic/anaphylactic response will be induced following administration of cells. A possible reaction between treated cells and T cells from recipient patient in-vitro can be tested by a mixed lymphocyte reaction prior to the study in healthy donors and MS patients. These assays document proliferation as well as cytokine release.

Proliferation assays against the antigen used in the trial will generate short term TCL. These antigen-specific T cells are co-cultured with autologous ECDI fixed antigen coupled APC in a 24 well culture plate at 37° C. in 5% CO₂ at a ratio of 1:1 to 1:2 (T:APC) with total 2-4×10⁶ total mixed cells. After 24 h cultured cell mixtures are collected and applied to a Ficoll gradient to isolate viable cells. After washing in culture medium (RPMI 1640) live cells are remixed with antigen in the presence of APC and evaluated for proliferation, activation status by FACS, cytokine secretion (IL-2, IL-4, IFN-g, IL-17) and cytokine mRNA expression. Depending on the timing of restimulation, one might expect anergy induction and/or induction of activation-induced cell death (AICD). Such cases should be properly documented.

The objective of this study was to evaluate the effect of peptide-coupled PBMC on immune activation of PBMC in-vitro. PBMC from MS patients (n=2) and a healthy control were cultured in the presence of peptide-coupled PBMC and analysed for proliferation response by thymidine incorporation and cytokine secretion (IL12, IFN-γ, IL10, IL1β, TNF-α) using a FACS based array (FlowCytomix, Bendermedsystems).

To assess cell proliferation in response to peptide-coupled cells, PBMC were seeded in two 96 well plates at 1×10⁵ cells/well in complete IMDM containing 100 U/ml penicillin/streptomycin, 50 μg/ml gentamicin, 2 mM L-gutamine, 5% heat decomplemented human serum. To the respective wells, either 5×10⁴ PBMC treated with EDC in the presence of the 7 peptides used in the trial (=peptide-coupled PBMC, tAPCpep), 5×10⁴ PBMC treated with EDC but without peptide (tAPC), 2.5 μg/ml phytohhaemagglutinin (PHA) or without further stimulus (APC) were added.

Presence of peptide-coupled cells did not induce proliferation in PBMC compared to unstimulated PBMC or PHA stimulated PBMC (FIG. 3).

The presence of inflammatory cytokines after 3 h and 24 h was also analyzed. Briefly, PBMC were cultured overnight in complete IMDM containing 100 U/ml penicillin/streptomycin, 50 μg/ml gentamicin, 2 mM L-gutamine, 5% heat decomplemented human serum, either in the presence of 2.5 μg/ml PHA or without stimulus. After 24 h, cells were washed in complete IMDM and seeded in a 24 well plate (4×10⁶/ml) in the presence of either PBMC treated with EDC and 7 peptides used in the trial (=peptide-coupled PBMC, tAPCpep), 1×10⁶ PBMC treated with EDC but without peptide (tAPC), 2.5 μg/ml PHA (PHA) or without further stimulus (APC).

As depicted in FIG. 4 and FIG. 5 there is no significant induction of inflammatory cytokines in the presence of peptide-coupled PBMC compared to the negative control (APC).

Depicted in FIG. 5 are the concentrations of cytokines without PHA control.

To analyze whether the response to peptide coupled cells differs dependent on the activation status of the cells, PBMC were pre-activated with PHA for 24 h and added the peptide-coupled PBMC. There was no induction of proliferation (FIG. 6) or cytokines (FIG. 7) in response to peptide-coupled cells.

In summary, the presence of peptide-coupled cells in-vitro did not induce activation of immune cells. These results correlate well with the results on the tolerization of human T-cell clones in-vitro and the induction of tolerance with peptide-coupled cells in-vivo in different animal models (34).

Potency of Human Peptide Coupled Cells In-Vitro

The objective of the study was to evaluate the effect of peptide-coupled cells on the antigen-specific response of human T cells. A T-cell clone (TCC) obtained from the cerebrospinal fluid (CSF) of an MS patient during relapse was used. Briefly, TCC (2×10⁴ cells/well) was cultured in complete IMDM (containing 100 U/ml penicillin/streptomycin, 50 μg/ml gentamicin, 2 mM L-gutamine, 5% heat decomplemented human serum) and pulsed with the peptide (MSI118) in the presence of irradiated PBMC (1×10⁵ cells/well). Peptide (MSI118, 10 μg/ml) coupled PBMC were added to the wells at different cell concentrations. Proliferative response of the TCC was measured by ³H-Thymidine incorporation after 72 h (FIG. 8).

Incubation of TCC with the specific peptide in the presence of antigen-coupled cells reduces the antigen specific response measured by thymidine incorporation in a dose-dependent manner.

To exclude a toxic inhibition of the peptide-coupled cells on the TCC, IL-2 or anti-CD28 monoclonal antibody were added to respective wells. As depicted in FIG. 9, proliferation of the TCC can be recuperated by the addition of either IL-2 or the anti-CD28 antibody in the presence of peptide-coupled cells.

It has been suggested that by fixing peptide pulsed antigen presenting cells a immunologic synapse cannot be formed and anergy is induced in autoreactive T-cells through presentation of the peptide through the MHC without co-stimulation. The immunologic synapse refers to the spatially organized motif of membrane proteins and cytosolic molecules that forms at the junction between T cell and an antigen presenting cell.

To further explore the invention, the formation of the immunologic synapse is analyzed by fluorescence microscopy and by analyzing the biophysical parameters (e.g. calcium influx) characterizing TCR MHC interaction.

Until now it is not clear from the literature, neither from the animal model, nor human studies, which subset of antigen presenting cells is most important in the tolerization process. This question was examined by analyzing the potency of the regimen as described above, after isolating specific cells from the PBMC population. Isolation of cells is performed using columns with labelled beads or a cell sorter.

Comparable results may be achieved on the basis of red blood cells (erythrocytes) chemically coupled with one of the cocktails of peptides defined herein. It is clear that in case of red blood cells the step of erythrocyte lysis has to be avoided and that cell-collection procedures have to be adapted accordingly.

DEFINITION OF MYELIN PEPTIDES

The myelin peptides specifically disclosed in this application are characterized by the following sequences:

MBP₁₃₋₃₂ (SEQ ID NO: 1):  KYLATASTMDHARHGFLPRH MBP₈₃₋₉₉ (SEQ ID NO: 2):  ENPVVHFFKNIVTPRTP MBP₁₁₁₋₁₂₉ (SEQ ID NO: 3):  LSRFSWGAEGQRPGFGYGG MBP₁₄₆₋₁₇₀ (SEQ ID NO: 4):  AQGTLSKIFKLGGRDSRSGSPMARR PLP₁₃₉₋₁₅₄ (SEQ ID NO: 5):  HCLGKWLGHPDKFVGI MOG₁₋₂₀ (SEQ ID NO: 6):  GQFRVIGPRHPIRALVGDEV MOG₃₅₋₅₅ (SEQ ID NO: 7):  MEVGWYRPPFSRVVHLYRNGK MBP₈₂₋₉₈ (SEQ ID NO: 8):  DENPVVHFFKNIVTPRT MBP₈₂₋₉₉ (SEQ ID NO: 9):  DENPVVHFFKNIVTPRTP MBP₈₂₋₁₀₆ (SEQ ID NO: 10): DENPVVHFFKNIVTPRTPPPSQGK MBP₈₇₋₁₀₆ (SEQ ID NO: 11): VHFFKNIVTPRTPPPSQGK MBP₁₃₁₋₁₅₅ (SEQ ID NO: 12): ASDYKSAHKGLKGVDAQGTLSKIFK PLP₄₁₋₅₈ (SEQ ID NO: 13): GTEKLIETYFSKNYQDYE PLP₈₉₋₁₀₆ (SEQ ID NO: 14): GFYTTGAVRQIFGDYKTT PLP₉₅₋₁₁₆ (SEQ ID NO: 15): AVRQIFGDYKTTICGKGLSATV PLP₁₇₈₋₁₉₇ (SEQ ID NO: 16): NTWTTCQSIAFPSKTSASIG PLP₁₉₀₋₂₀₉ (SEQ ID NO: 17): SKTSASIGSLCADARMYGVL MOG₁₁₋₃₀ (SEQ ID NO: 18): PIRALVGDEVELPCRISPGK MOG₂₁₋₄₀ (SEQ ID NO: 19): ELPCRISPGKNATGMEVGWY MOG₆₄₋₈₆ (SEQ ID NO: 20): EYRGRTELLKDAIGEGKVTLRIR PLP (human) full length protein  SEQ ID NO: 21 MGLLECCARCLVGAPFASLV ATGLCFFGVALFCGCGHEALTGTEKLIET YFSKNYQDYEYLINVIHAFQYVIYGTASFFFLYGALLLAEGFYTTGAVRQ IFGDYKTTICGKGLSATVTGGQKGRGSRGQHQAHSLERVCHCLGKWLGHP DKITYALTVVWLLVFACSAVPVYIYFNTWTTCQSIAFPSKTSASIGSLCA DARMYGVLPWNAFPGKVCGSNLLSICKTAEFQMTFHLFIAAFVGAAATLV SLLTFMIAATYNFAVLKLMGRGTKF MBP (human) full length protein (18.5Kd isoform) SEQ ID NO: 22 ASQKRPSQRHGSKYLATASTMDHARHGFLPRHRDTGILDSLGRFFGGDRG APKRGSGKDSHHAARTTHYGSLPQKSHGRTQDENPVVHFF KNIVTPRTPPPSQGKGRGLSLSRFSWGAEGQRPGFGYGGRASDYKSAHKG LKGVDAQGTLSKIFKLGGRD SRSGSPMARR MOG (human) full length protein SEQ ID NO: 23 MASLSRPSLPSCLCSFLLLLLLQVSSSYAGQFRVIGPRHPIRALVGDEVE LPCRISPGKNATGMEVGWYRPPFSRVVHLYRNGKDQDGDQAPEYRGRTEL LKDAIGEGKVTLRIRNVRFSDEGGFTCFFRDHSYQEEAAMELKVEDPFYW VSPGVLVLLAVLPVLLLQITVGLVFLCLQYRLRGKLRAEIENLHRTFDPH FLRVPCWKITLFVIVPVLGPLVALIICYNWLHRRLAGQFLEELRNPF Specific Citrullinated Sequences (See Lit. ref. 46, below): MBP₁₈₋₃₈ (Cit) (SEQ ID NO: 24): ASTMDHACitHGFLPCitHRDTGIL MBP₁₁₅₋₁₃₁ (Cit) (SEQ ID NO: 25): SWGAEGQCitPGFGYGGCitA MBP₁₅₁₋₁₇₀ (Cit) (SEQ ID NO: 26): SKIFKLGGCitDSRSGSPMARR

The sequences defined above include different end modifications of the peptides, e.g. acetylation, amidation, carboxylation.

EXAMPLE

1.5-2×10⁹ peripheral blood mononuclear cells are isolated from a MS patient. The isolated cells are coupled according to the manufacture process described above with a cocktail of the following peptides MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₁₄₆₋₁₇₀, PLP₁₃₉₋₁₅₄, MOG₁₋₂₀ and MOG₃₅₋₅₅. The resulting suspension of approximately 10⁹ cells suspended in 100 ml water buffered to pH 7.2-7.8 is infused intravenously to the patient. MRI examinations carried out before and after application (e.g. 1 day, 1 week, 1 month, 6 months, 1 year after application) convincingly demonstrates the efficacy of the procedure in terms of reduction of CNS-inflammation. The MRI findings are in line with other clinical symptoms.

It will be appreciated by the expert skilled in the art that the description relating to the manufacturing process (including all tests and validation steps) are provided as examples. They are not meant to limit the invention in any way. The expert skilled in the art will certainly be able to carry out the invention as described above but also to modify the invention in various aspects based on his general knowledge without any need to be inventive.

LITERATURE REFERENCES

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All of the references cited above are incorporated herein by reference. 

1-20. (canceled)
 21. A chemically coupled cell which is a peripheral blood mononuclear cell (PBMC) or a red blood cell erythrocyte that is chemically coupled to a cocktail of peptides which cocktail comprises at least five peptides out of the following peptides: MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆.
 22. A chemically coupled cell which is a peripheral blood mononuclear cell (PBMC) or a red blood cell erythrocyte that is chemically coupled to a cocktail of peptides which cocktail comprises at least six peptides out of the following peptides: MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆.
 23. A chemically coupled cell which is a peripheral blood mononuclear cell (PBMC) or a red blood cell that is chemically coupled to a cocktail of peptides which cocktail comprises at least one of cocktails e-oo of tables 5.1-5.3.
 24. The chemically coupled cell according to claim 23, wherein a MBP peptide is replaced with the full length MBP protein.
 25. The chemically coupled cell according to claim 24, wherein the full length MBP protein is the 18.5 kD isoform according to SEQ ID NO:
 22. 26. The chemically coupled cell according to claim 23, wherein a MBP peptide is citrullinated.
 27. The chemically coupled cell according to claim 23, wherein a PLP peptide is replaced with the full length PLP protein according to SEQ ID NO:
 21. 28. The chemically coupled cell according to claim 23, wherein a MOG peptide is replaced with the full length MOG protein according to SEQ ID NO:
 23. 29. The chemically coupled cell according to claim 21, which is a red blood cell.
 30. The chemically coupled cell according to claim 21, which is a peripheral blood mononuclear cell.
 31. The chemically coupled cell according to claim 21, wherein the peptides are chemically coupled by 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDCI).
 32. A pharmaceutical composition comprising chemically coupled cell according to one of claim 21 and an excipient.
 33. A medical product comprising chemically coupled cell according to claim 21 and an anti-coagulant.
 34. A method for the treatment of an autoimmune inflammatory disease in a subject in need thereof, comprising administering into said subject chemically coupled cells according to claim
 21. 35. The method according to claim 24, wherein the autoimmune inflammatory disease is Multiple Sclerosis (MS).
 36. The method according to claim 24, wherein the chemically coupled cells are allogenic relative to said subject.
 37. The method according to claim 24, wherein the chemically coupled cells are autologous relative to said subject.
 38. A process for the manufacture of a cell according to claim 21, comprising contacting said cell with at least comprises at least five peptides out of the following group of peptides comprising: MBP₁₃₋₃₂, MBP₈₃₋₉₉, MBP₁₁₁₋₁₂₉, MBP₈₂₋₉₈, MBP₈₂₋₉₉, MBP₈₂₋₁₀₆, MBP₈₇₋₁₀₆, MBP₁₃₁₋₁₅₅, MBP₁₄₆₋₁₇₀, PLP₄₁₋₅₈, PLP₈₉₋₁₀₆, PLP₉₅₋₁₁₆, PLP₁₃₉₋₁₅₄, PLP₁₇₈₋₁₉₇, PLP₁₉₀₋₂₀₉, MOG₁₋₂₀, MOG₁₁₋₃₀, MOG₂₁₋₄₀, MOG₃₅₋₅₅, MOG₆₄₋₈₆ in the presence of a coupling agent.
 39. A process for the manufacture of a cell according to claim 23, comprising contacting said cell with at least one of said cocktail of peptides e-oo in the presence of a coupling agent.
 40. The process according to claim 38, wherein the coupling agent is 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDCI). 